Bariatric surgery-induced weight loss in morbidly obese patients promotes a favorable decrease in the gene expression of markers of subcutaneous adipose tissue homeostasis

2016 ◽  
Vol 252 ◽  
pp. e221
Author(s):  
J. Julve ◽  
E. Pardina ◽  
R. Ferrer ◽  
J. Rossell ◽  
J.A. Baena-Fustegueras ◽  
...  
1986 ◽  
Vol 20 (11) ◽  
pp. 869-873 ◽  
Author(s):  
Henry J. Mann ◽  
Henry Buchwald

Distribution and elimination of cefamandole 2 g iv were studied in 11 morbidly obese patients during a gastric bypass operation and again on the first postoperative day. Serum, subcutaneous adipose tissue, wound drainage, and urine were analyzed by high performance liquid chromatography for cefamandole and pharmacokinetic parameters from the intraoperative period were compared to those obtained postoperatively. Total body clearance was significantly greater (p < 0.001) postoperatively (297 ml/min) than intraoperatively (254 ml/min). Volume changes were unpredictable but the elimination rate constant tended to increase postoperatively. Renal clearance and percentage of urinary recovery were significantly increased (p < 0.01) postoperatively. The patients had a mean (± SD) volume of the central compartment of 10.3 (± 2.3) L, volume at steady state of 18.3 (± 3.9) L, and elimination rate constant of 1.67 (± 0.63) h−1. Tissue concentrations of cefamandole were highest during the first hour after drug administration and were < 1 μg/g after 3.5 hours. Mean wound drainage concentrations ranged between 10 and 12 μg/ml during a dosing interval and dropped to 7 μg/ml 12 hours after the last dose. Intraoperative dosing of cefamandole is required to maintain subcutaneous adipose tissue concentrations > 1 μg/g during procedures longer than three hours in morbidly obese patients. A postoperative dose of cefamandole 2 g iv q6h will provide sustained and therapeutic concentrations in the wound drainage of morbidly obese patients.


2016 ◽  
Vol 73 ◽  
pp. 53-59 ◽  
Author(s):  
Fusun Ozmen ◽  
M. Mahir Ozmen ◽  
Sibel Gelecek ◽  
İsmail Bilgic ◽  
Munevver Moran ◽  
...  

2016 ◽  
Author(s):  
Sara Garcia-Serrano ◽  
Carolina Gutierrez-Repiso ◽  
Francisca Rodriguez-Pacheco ◽  
Ailec Ho-Plagaro ◽  
Eva Garcia-Escobar ◽  
...  

2008 ◽  
Vol 19 (6) ◽  
pp. 764-770 ◽  
Author(s):  
Rodrigo Muñoz ◽  
Cristian Carvajal ◽  
Alex Escalona ◽  
Camilo Boza ◽  
Gustavo Pérez ◽  
...  

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Ronald Biemann ◽  
Kirsten Roomp ◽  
Fozia Noor ◽  
Shruthi Krishnan ◽  
Zhen Li ◽  
...  

Abstract Lifestyle-induced weight loss is regarded as an efficient therapy to reverse metabolic syndrome (MetS) and to prevent disease progression. The objective of this study was to investigate whether lifestyle-induced weight loss modulates gene expression in circulating monocytes. We analyzed and compared gene expression in monocytes (CD14+ cells) and subcutaneous adipose tissue biopsies by unbiased mRNA profiling. Samples were obtained before and after diet-induced weight loss in well-defined male individuals in a prospective controlled clinical trial (ICTRP Trial Number: U1111-1158-3672). The BMI declined significantly (− 12.6%) in the treatment arm (N = 39) during the 6-month weight loss intervention. This was associated with a significant reduction in hsCRP (− 45.84%) and circulating CD14+ cells (− 21.0%). Four genes were differentially expressed (DEG’s) in CD14+ cells following weight loss (ZRANB1, RNF25, RB1CC1 and KMT2C). Comparative analyses of paired CD14+ monocytes and subcutaneous adipose tissue samples before and after weight loss did not identify common genes differentially regulated in both sample types. Lifestyle-induced weight loss is associated with specific changes in gene expression in circulating CD14+ monocytes, which may affect ubiquitination, histone methylation and autophagy.


Obesity Facts ◽  
2012 ◽  
Vol 5 (3) ◽  
pp. 440-451 ◽  
Author(s):  
Céline Leyvraz ◽  
Chantal Verdumo ◽  
Michel Suter ◽  
Alexandre Paroz ◽  
Jean-Marie Calmes ◽  
...  

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